Abstract
Background
Intensive residential treatment (IRT) is effective for severe, treatment-resistant obsessive-compulsive disorder (OCD). We sought to characterize predictors and course of response to IRT.
Methods
Admission, monthly, and discharge data were collected on individuals receiving IRT. We examined the association between baseline characteristics and percent change in OCD symptoms as measured by the Yale-Brown Obsessive-Compulsive Scale (Y-BOCS) using linear regression. We compared baseline characteristics of IRT responders (≥35% reduction in Y-BOCS) versus non-responders, and of patients who did versus those who did not achieve wellness (Y-BOCS ≤12) using non-parametric tests. To examine the course of OCD severity over time, we used linear mixed-effects models with randomly varying intercepts and slopes.
Results
We evaluated 281 individuals admitted to an IRT program. Greater baseline Y-BOCS scores were associated with a significantly greater percent reduction in Y-BOCS scores (β = −1.49 ([95% confidence interval: −2.06 to −0.93]; P<.001). IRT responders showed significantly greater baseline Y-BOCS scores than non-responders (mean (SD) 28 (5.2) vs. 25.6 (5.8); P=.003) and lower past-year alcohol use scores than non-responders (1.4 (1.9) vs. 2.1 (2.2); P=.01). Participants who achieved wellness displayed lower hoarding factor scores than those who did not (5 (4.6) vs. 9.53 (6.3); P=.03). OCD symptoms declined rapidly over the first month but more slowly over the remaining two months.
Conclusions
Higher baseline OCD severity, lower past-year alcohol use, and fewer hoarding symptoms predicted better response to IRT. IRT yielded an initial rapid reduction in OCD symptoms, followed by a slower decline after the first month.
Keywords: obsessive-compulsive disorder, OCD, intensive residential treatment, IRT, predictors, hoarding
BACKGROUND
Obsessive-compulsive disorder (OCD) is a chronic and often debilitating psychiatric illness, affecting between 2% and 3% of the United States population at some time in their lives (Karno et al., 1988). The current first-line treatments for OCD include both pharmacologic approaches such as the selective serotonin reuptake inhibitors and behavioral treatment such as exposure response prevention therapy. For most OCD patients, these treatments alone or in combination produce at least moderate symptom reduction (Jenike, 2004). However, a subset of OCD patients derives little or no relief from these therapies and requires more intensive treatment approaches. This severe, treatment-refractory subset of cases accounts for nearly all of the OCD-related psychiatric hospitalizations in the United States, as well as the vast majority of social and functional impairment (Ruscio et al., 2010). Thus, it is important to develop specialized treatment approaches targeting this unique and challenging patient population.
One such approach is intensive residential treatment (IRT). IRT utilizes a multidimensional treatment strategy incorporating intensive behavioral, medication, and milieu treatment administered in a residential setting. To date, several studies of IRT have demonstrated a significant reduction in OCD symptoms (Bjorgvinsson et al., 2013; Bjorgvinsson et al., 2008; Boschen et al., 2008; Drummond, 1993; Stewart et al., 2005) that persists post-discharge (Stewart et al., 2009), suggesting that this approach is a viable treatment option for OCD patients with severe and refractory illness. However, given the significant personal and financial investment required for IRT, it is important to seek predictors of response to this treatment. Currently, three studies of IRT have examined outcome predictors for patients with OCD (Bjorgvinsson et al., 2013; Bjorgvinsson et al., 2008; Stewart et al., 2006), but two of these (Bjorgvinsson et al., 2013; Bjorgvinsson et al., 2008) employed modest sample sizes (N < 50) and one (Bjorgvinsson et al., 2008) examined only adolescents with OCD. Moreover, none of these studies examined the longitudinal course of treatment response. Such studies are critical for refining and optimizing the IRT approach.
The Obsessive-Compulsive Disorder Institute at McLean Hospital (OCDI), a representative IRT program, utilizes a multidisciplinary staff to provide intensive behavioral, pharmacologic, and group treatment at both residential and partial hospital levels of care. On average, IRT involves about 2–4 hours of daily exposure response prevention therapy, weekly meetings with psychiatrists who specialize in the pharmacologic management of OCD, and case management with a social worker to address family dynamics and aftercare planning. The average length of stay in the OCDI is approximately 45 days, and about 25% of patients stay at least 3 months.
In a previous study of OCDI patients, our group found that lower initial OCD severity, female sex, and better baseline psychosocial functioning predicted less severe OCD at discharge (Stewart et al., 2006). However, this study did not examine the trajectory of OCD severity over the course of IRT – data that could guide decisions on optimal treatment approaches and length of stay. Therefore, the aims of this study were 1) to replicate and expand upon our previous findings of baseline predictors of response to IRT and 2) to characterize the course of OCD severity over time during IRT treatment. Based on our previous study, we hypothesized that female patients with less severe OCD, better baseline psychosocial functioning, and fewer baseline depressive symptoms would respond best to IRT. We also hypothesized that patients with primary contamination/washing symptoms would respond better to IRT than other patients, since in our experience, contamination/washing symptoms generally appear more amenable to the exposure response prevention approach. Additionally, based on anecdotal experience, we hypothesized that patients receiving IRT improve rapidly over the first month, but more gradually thereafter.
MATERIALS AND METHODS
Study Population
Study participants were first time-admissions to the OCDI between May 2011 and May 2013 who gave written informed consent to participate in a research database study approved by the McLean Hospital Institutional Review Board. Each participant met admission criteria to the OCDI, which included having severe OCD symptoms, significantly compromised social and occupational functioning, and evidence of treatment resistance to previous medication trials or outpatient behavioral therapies. In addition, each patient had a confirmed diagnosis of OCD based on admission assessments by both a behavioral therapist and a psychiatrist with expertise in OCD.
Clinical Assessments
Each study participant was administered a battery of self-report clinical rating scales upon admission, detailed below, which were repeated monthly and at discharge. Participants also completed an admission demographic questionnaire covering age of onset of OCD symptoms, family history of OCD, marital status, educational background, employment status, and prior diagnosis of post-traumatic stress disorder.
The Yale-Brown Obsessive Compulsive Scale (Y-BOCS), our primary measure of OCD severity, is a 10-item scale with demonstrated reliability used to assess the severity of both obsessions and compulsions, with each item rated on a scale between 0 (lowest severity) and 4 (highest severity) (Goodman et al., 1989). The self-report version of the Y-BOCS has been shown to correlate highly with the clinician-administered version (Federici et al., 2010). The Obsessive Compulsive Symptoms Rating Scale (OCSRS) is a self-report measure that assesses the presence of 67 specific OCD and obsessive-compulsive spectrum symptoms grouped into 22 categories including obsessions (e.g., aggression, contamination, sexual, hoarding, religious, symmetry, somatic), compulsions (e.g., cleaning, checking, repeating, counting, ordering, hoarding), and several miscellaneous categories (Wilhelm and Steketee, 2006). Individuals then rate the severity of each category on a scale from 0 (no problem) to 10 (very severe). These category scores have been shown to be reliable and valid with good internal consistency (Yovel et al., 2012). The Quick Inventory of Depressive Symptomatology – Self Report Version (QIDS-SR16), a widely used 16-item self-report scale with demonstrated high internal consistency and validity (Rush et al., 2003), assesses the severity of depressive symptoms. The Work and Social Adjustment Scale (WSA), a 5-item self-report measure of functional impairment, demonstrates good reliability and validity (Mundt et al., 2002) Each item is rated on a scale from 0 (not at all) to 8 (very severe). The 10-item Schwartz Outcome Scale (SOS-10) is a reliable and internally consistent (Blais et al., 1999) quality-of-life measure with higher scores indicating better functioning. The Alcohol Use Disorders Identification Test – Consumption Questions (AUDIT-C), and the Drug Abuse Screening Test (DAST-10) are brief screening questionnaires with demonstrated reliability and face validity (Bush et al., 1998; Skinner, 1982) assessing past-year alcohol and drug use, respectively, with higher scores indicating greater evidence of abuse or dependence.
Using established criteria (Farris et al., 2013), we defined “response” as a decrease in Y-BOCS score of ≥ 35% from admission to discharge and “wellness” as a Y-BOCS score of ≤ 12 at last assessment. For participants discharged before discharge measures could be obtained, we used the final completed assessment in a last-observation-carried-forward (LOCF) approach.
Statistical Analyses
Univariate Predictors of Response and Wellness
We examined the association between baseline characteristics and percent change in total Y-BOCS scores between admission and discharge assessments using linear regression. Additionally, we compared the baseline characteristics of responders versus non-responders, and of patients who did and did not achieve wellness, using the Wilcoxon rank-sum test for continuous data and Fisher’s exact test for categorical data. All baseline characteristics of interest were chosen prior to conducting any analyses and all results (both significant and non-significant) are reported in this manuscript.
We also assessed OCD symptom dimension ratings, obtained at admission, as predictors of response. Using the widely accepted four-factor solution for OCD symptoms, which includes: 1) forbidden thoughts (aggressive, sexual, and religious obsessions) and checking compulsions; 2) symmetry obsessions and ordering compulsions; 3) contamination obsessions and washing compulsions; and 4) hoarding obsessions and compulsions, (Bloch et al., 2008) we calculated factor scores for each of the four factor domains by adding the symptom category ratings within each factor. Only observations with factor scores greater than zero were considered in the analysis. For each factor dimension, the correlation between factor scores and percent change in Y-BOCS was calculated and the factor scores for responders versus non-responders and for those who achieved wellness versus those who did not were compared.
Modeling the Course of OCD Severity Over Time
To model the course of OCD severity over time, we considered a random intercept and slope (RIS) model for the trajectory of total Y-BOCS over time adjusted for age and sex, where the model is given by:
where b0i is the random intercept, b1i is the random slope, and ξij is the random within-subject error, for subjects numbered i = 1, …, 287 with assessments j = 1, …, ni, where the maximum number of assessments ni varies by patient and can take on values from 1 to 4. Quadratic fixed effects were then added to the above models, followed by cubic effects. Quadratic and cubic random effects were not considered due to over-fitting, since subjects in the dataset had a maximum of four assessments, and a majority had two assessments or fewer (see results below). Secondary analyses were conducted using transformations of time, specifically log(time + 1) and √time, to assess model fit.
Finally, we performed exploratory analyses using non-parametric methods to better understand the relationship between OCD severity and time. First, we used locally weighted scatterplot smoothing (LOESS) to fit curves of varying smoothness through the scatterplot of Y-BOCS scores versus time since admission. Next, we used penalized smoothing (linear splines for longitudinal data) to model the trajectory of OCD severity, taking into consideration the within-subject variability of the repeated assessments. The latter models were fitted taking knots at every 5, 10, 20, and 30 days. Last, to investigate the possible relationship between length of stay and OCD severity trajectory, we compared the profile plots of participants whose last assessments were at least 30 days post-admission. We did the same for participants whose last assessments were at least 45, 60, and 75 days post-admission.
RESULTS
Baseline Characteristics
We assessed 287 patients admitted for the first time to the OCDI between May 2011 and May 2013. Six of these patients were removed from the analysis for having admission Y-BOCS scores below the wellness criterion (≤ 12). Baseline characteristics of the sample are presented in Table 1. Over half (56%) of participants had received prior treatment with a combination of behavioral therapy and medications, and an additional 32% reported receiving either behavioral therapy (14%) or medications (18%) prior to admission. Despite this, participants typically reported severe and debilitating symptoms at admission, as indicated by initial Y-BOCS scores (mean (SD) 26.7 (5.6)) and WSA scores (mean 27.3 (7.7)), implying a high degree of treatment-refractoriness.
TABLE 1.
Characteristic | N (%) | Mean (SD) | Range |
---|---|---|---|
Age, years (N = 281) | 33.5 (13.8) | 16–78 | |
Sex (N = 281) | |||
Male | 143 (51) | ||
Female | 138 (49) | ||
Education (N = 274) | |||
High School Diploma/GED | 88 (32) | ||
Some College or Associates Degree | 57 (21) | ||
Bachelors Degree | 89 (32) | ||
Graduate Degree | 40 (15) | ||
Employment (N = 275) | |||
Employed | 81(29) | ||
Unemployed or On Leave | 194 (71) | ||
Marital status (N = 275) | |||
Single | 202 (73) | ||
Married or Partner | 54 (20) | ||
Divorced or Separated | 19 (7) | ||
Payment method (N = 275) | |||
Managed care | 215 (78) | ||
Medicare/Medi-caid | 48 (18) | ||
Self-pay | 12 (4) | ||
Past treatment (N = 270) | |||
Behavioral therapy | 38 (14) | ||
Medication | 49 (18) | ||
Behavioral therapy and medication | 151 (56) | ||
Other treatment method | 18 (7) | ||
Never received treatment | 14 (5) | ||
Age of OCD Onset, years (N = 235) | 14.3 (9.6) | 0–61 | |
Duration of OCD, years (N = 235) | 18.8 (13.4) | 1–64 | |
Yale-Brown Obsessive Compulsive Scale (N = 281) | 26.7 (5.6) | 13–40 | |
Quick Inventory of Depressive Symptomatology (N = 280) | 13.3 (5.4) | 1–26 | |
Work and Social Adjustment Scale (N = 204) | 27.3 (7.7) | 0–40 | |
Schwartz Outcome Scale (N = 204) | 23.6 (10.5) | 0–54 | |
Time between admission and last assessment, days (N = 223) | 52.5 (22.7) | 6–101 |
Of the initial 281 participants analyzed, 58 (21%) had admission data only, 101 (36%) had admission data with one follow-up assessment, 87 (31%) had two follow-up assessments, and 35 (12%) had three follow-up assessments. Discharge measures were obtained on 202 out of the initial 281 participants (72%).
Predictors of Response and Wellness
Of the various baseline characteristics analyzed (Table 2), only baseline Y-BOCS scores significantly predicted percent change in Y-BOCS at discharge (β = −1.49 ([95% confidence interval: −2.06, −0.93]; P <.001; effect size = −2.79 (slope/MSE)); however, some caution must be exercised in interpreting this association because there is necessarily a part-whole (negative) relationship between baseline and change. On the same characteristics, responders showed significantly greater baseline Y-BOCS scores (P = .003; effect size = 0.43 ((difference of sample means)/(pooled SD)) and lower AUDIT-C scores (P = .01; effect size = 0.34 ((difference of sample means)/pooled SD)), but did not differ significantly on any other characteristics (Table 3). There were no significant differences between participants who achieved wellness and participants who failed to achieve wellness (Table 4).
Table 2.
Characteristic | Slope | Slope SE | Slope p-value | Slope 95% CI |
---|---|---|---|---|
Age | 0.06 | 0.12 | 0.64 | (−0.18, 0.30) |
Age of OCD onset | −0.12 | 0.18 | 0.50 | (−0.47, 0.23) |
Alcohol Use Disorders Test - Consumption | 1.59 | 0.84 | 0.06 | (−0.06, 3.24) |
Drug Abuse Screening Test-10 | −0.06 | 1.36 | 0.96 | (−2.75, 2.62) |
Yale-Brown Obsessive Compulsive Scale | −1.49 | 0.29 | <.001 | (−2.06, −0.93) |
Quick Inventory of Depressive Symptomatology-16 | 0.42 | 0.32 | 0.19 | (−0.21, 1.04) |
Work and Social Adjustment Scale | −0.13 | 0.27 | 0.64 | (−0.66, 0.41) |
Schwarz Outcome Scale, 10 item | −0.17 | 0.19 | 0.37 | (−0.55, 0.21) |
Duration of illness | −0.06 | 0.14 | 0.69 | (−0.34, 0.22) |
Male | 2.50 | 3.42 | 0.47 | (−4.25, 9.24) |
Married/partner | −6.82 | 4.43 | 0.13 | (−15.56, 1.92) |
Currently employed | −1.14 | 3.74 | 0.76 | (−8.51, 6.23) |
Family history of OCD | −0.30 | 3.48 | 0.93 | (−7.16, 6.55) |
History of posttraumatic stress disorder | −7.33 | 5.72 | 0.20 | (−18.6, 3.95) |
Payment methoda | ||||
Managed care | −7.6 | 9.21 | 0.41 | (−25.8, 10.5) |
Medicare/Medi-caid | −9.0 | 9.98 | 0.37 | (−28.7, 10.7) |
Past treatmentb | ||||
Behavioral therapy | −1.20 | 8.60 | 0.89 | (−18.1, 15.8) |
Medication | 0.71 | 8.60 | 0.94 | (−16.2, 17.7) |
Behavioral therapy and medication | −2.14 | 7.78 | 0.78 | (−17.5, 13.2) |
Other treatment method | 3.75 | 9.67 | 0.70 | (−15.3, 22.8) |
Educationc | ||||
Some college or Associates degree | 4.88 | 4.93 | 0.32 | (−4.85, 14.6) |
Bachelors degree | −0.84 | 4.19 | 0.84 | (−9.1, 7.42) |
Graduate degree | −9.77 | 5.42 | 0.07 | (−20.5, 0.91) |
Reference group = Self-pay
Reference group = Never received treatment
Reference group = High school diploma or GED
Table 3.
Characteristic | Non-responders (N = 110)
|
Responders (N = 113)
|
p-value | ||
---|---|---|---|---|---|
N | Mean (SD) | N | Mean (SD) | ||
Age | 110 | 33.4 (14.5) | 113 | 33.4 (13.4) | 0.81 |
Age of OCD onset | 88 | 13.6 (7.9) | 98 | 15.6 (12.1) | 0.53 |
Alcohol Use Disorders Test - Consumption | 108 | 2.1 (2.2) | 109 | 1.4 (1.9) | 0.01 |
Drug Abuse Screening Test-10 | 110 | 0.8 (1.0) | 113 | 0.8 (1.5) | 0.33 |
Yale-Brown Obsessive Compulsive Scale | 110 | 25.6 (5.8) | 113 | 28 (5.2) | 0.003 |
Quick Inventory of Depressive Symptoms-16 | 110 | 13.6 (5.3) | 113 | 13.4 (5.5) | 0.81 |
Work and Social Adjustment scale | 84 | 26.9 (7.9) | 76 | 28.1 (7.3) | 0.3 |
Schwartz Outcome Scale-10 | 84 | 24.6 (11.4) | 76 | 22.5 (10.2) | 0.15 |
Duration of illness | 88 | 18.8 (13.8) | 98 | 18.2 (12.4) | 0.96 |
| |||||
Characteristic | N | N (%) | N | N (%) | p-value |
| |||||
Male | 110 | 58 (52.7) | 113 | 60 (53.1) | 1 |
Married/partner | 108 | 15 (13.9) | 109 | 25 (22.9) | 0.12 |
Currently employed | 108 | 30 (27.8) | 109 | 37 (33.9) | 0.38 |
Family history of OCD | 108 | 56 (51.9) | 108 | 62 (57.4) | 0.49 |
PTSD history | 106 | 10 (9.4) | 108 | 12 (11.1) | 0.82 |
Payment method | |||||
Managed care | 108 | 86 (79.6) | 109 | 88 (80.7) | 0.87 |
Medicare/Medi-caid | 108 | 18 (16.7) | 109 | 17 (15.6) | 0.86 |
Self-pay | 108 | 4 (3.7) | 109 | 4 (3.7) | 1 |
Past treatment | |||||
Behavioral therapy | 106 | 16 (15.1) | 108 | 17 (15.7) | 1 |
Medication | 106 | 16 (15.1) | 108 | 17 (15.7) | 1 |
Behavioral therapy and medication | 106 | 59 (55.7) | 108 | 62 (57.4) | 0.89 |
Other treatment method | 106 | 9 (8.5) | 108 | 7 (6.5) | 0.61 |
Never received treatment | 106 | 6 (5.7) | 108 | 5 (4.6) | 0.77 |
Education | |||||
High school diploma or GED | 108 | 36 (33.3) | 109 | 36 (33.0) | 1 |
Some college or Associates degree | 108 | 24 (22.2) | 109 | 17 (15.6) | 0.23 |
Bachelors degree | 108 | 38 (35.2) | 109 | 35 (32.1) | 0.67 |
Graduate degree | 108 | 10 (9.3) | 109 | 21 (19.3) | 0.051 |
Table 4.
Characteristic | Wellness not acheived (N = 174)
|
Wellness achieved (N = 53)
|
p-value | ||
---|---|---|---|---|---|
N | Mean (SD) | N | Mean (SD) | ||
Age | 173 | 33.3 (14.1) | 50 | 33.7 (13.4) | 0.83 |
Age of OCD onset | 141 | 14.2 (9.2) | 45 | 16.1 (13.2) | 0.36 |
Alcohol Use Disorders Test - Consumption | 167 | 1.9 (2.1) | 50 | 1.4 (1.8) | 0.14 |
Drug Abuse Screening Test-10 | 173 | 0.8 (1.3) | 50 | 0.6 (1.2) | 0.38 |
Yale-Brown Obsessive Compulsive Scale | 173 | 27.1 (5.4) | 50 | 25.7 (6.5) | 0.16 |
Quick Inventory of Depressive Symptoms-16 | 173 | 13.8 (5.5) | 50 | 12.5 (4.9) | 0.11 |
Work and Social Adjustment scale | 130 | 27.6 (7.8) | 30 | 26.5 (7.1) | 0.46 |
Schwartz Outcome Scale-10 | 130 | 23.3 (10.8) | 30 | 25.1 (11.1) | 0.43 |
Duration of illness | 141 | 18.5 (13.4) | 45 | 18.2 (11.7) | 0.86 |
| |||||
Characteristic | N | N (%) | N | N (%) | p-value |
| |||||
Male | 173 | 92 (53.2) | 50 | 26 (52.0) | 1 |
Married/partner | 170 | 33 (19.4) | 47 | 7 (14.9) | 0.53 |
Currently employed | 170 | 53 (31.2) | 47 | 14 (29.8) | 1 |
Family history of OCD | 170 | 94 (55.3) | 46 | 24 (52.2) | 0.74 |
PTSD history | 168 | 14 (8.3) | 46 | 8 (17.4) | 0.1 |
Payment method | |||||
Managed care | 170 | 135 (79.4) | 47 | 39 (83.0) | 0.68 |
Medicare/Medi-caid | 170 | 27 (15.9) | 47 | 8 (17.0) | 0.83 |
Self-pay | 170 | 8 (4.7) | 47 | 0 (0) | 0.21 |
Past treatment | |||||
Behavioral therapy | 168 | 27 (16.1) | 46 | 6 (13.0) | 0.82 |
Medication | 168 | 26 (15.5) | 46 | 7 (15.2) | 1 |
Behavioral therapy and medication | 168 | 93 (55.4) | 46 | 28 (60.9) | 0.62 |
Other treatment method | 168 | 13 (7.7) | 46 | 3 (6.5) | 1 |
Never received treatment | 168 | 9 (5.4) | 46 | 2 (4.3) | 1 |
Education | |||||
High school diploma or GED | 170 | 55 (32.4) | 47 | 17 (36.2) | 0.73 |
Some college or Associates degree | 170 | 36 (21.2) | 47 | 5 (10.6) | 0.14 |
Bachelors degree | 170 | 59 (34.7) | 47 | 14 (29.8) | 0.60 |
Graduate degree | 170 | 20 (11.8) | 47 | 11 (23.4) | 0.058 |
None of the four dimensional factor scores was significantly associated with percent change in Y-BOCS scores (Table 5), nor did any factor scores differ significantly between responders and non-responders. However, participants who achieved wellness had significantly lower hoarding factor scores than participants who did not achieve wellness (P = .03; effect size = 0.94 ((difference of sample means)/pooled SD)) (Table 5).
Table 5.
Symptom dimension | Wellness not acheived
|
Wellness achieved
|
p-value | ||
---|---|---|---|---|---|
N | Mean factor score (SD) | N | Mean factor score (SD) | ||
Symmetry (N =109) | 56 | 11.1 (7.2) | 53 | 10.1 (8.3) | 0.36 |
Forbidden thoughts (N =134) | 110 | 15.2 (10.6) | 24 | 11.9 (10.1) | 0.07 |
Contamination (N =115) | 93 | 10.7 (5.9) | 22 | 11.2 (6.8) | 0.81 |
Hoarding (N =65) | 57 | 9.53 (6.3) | 8 | 5 (4.6) | 0.03 |
Time Course of OCD Severity
Goodness-of-fit tests suggested that the best-fitting model of time course was the RIS with cubic fixed effects, both when using transformed or untransformed time. Profile plots of 100 randomly selected participants showed similar trajectories for the three primary adjusted models (Figure 1) over the first 60 days, with the quadratic fixed effects model diverging from the others thereafter. Given the possibility that the trajectory after 60 days was strongly influenced by the small subset of patients staying for more than 60 days, we repeated the same analyses using data restricted to 60 days or less, but the curves remained virtually unchanged from the 90-day model. Therefore, further exploratory analyses using non-parametric methods were performed using data up to 90 days. Analyses using LOESS suggested that improvement occurred rapidly during the first 30 days but more gradually thereafter (Figure 2). Analyses using penalized smoothing with knots at 20 and 30 days yielded similar curves (Figure 3a and 3b). Penalized smoothing using knots of 5 and 10 days suggested a possible temporary spike in OCD symptoms from days 20–40 and another smaller brief spike around the 60-day mark (Figure 3c and 3d). Finally, when all of the time course analyses were repeated without adjustment for age and sex, they yielded identical results.
DISCUSSION
Outcome Predictors
We found that greater baseline OCD severity predicted greater percent reduction in OCD symptoms following IRT. Because some component of this association is due to “regression to the mean”, the clinical implications of this result must be interpreted with some care. Similarly, we found that IRT responders exhibited greater baseline OCD severity than non-responders. These findings accord with Bjorgvinsson et al. (Bjorgvinsson et al., 2008) who reported a similar association between greater baseline OCD severity and response to IRT in adolescents with OCD, but contrast with a later study by the same group in adults receiving IRT (Bjorgvinsson et al., 2013) and with our previous study (Stewart et al., 2006). Studies examining outpatients with OCD have consistently demonstrated an association between lower OCD severity and response to cognitive behavioral therapy (CBT) (Keeley et al., 2008; Knopp et al., 2013) and medication (Denys et al., 2003; Shetti et al., 2005; Stein et al., 2001; Storch et al., 2006; Tukel et al., 2006). Thus, our present findings suggest that inpatient IRT may be particularly suited for severe OCD although more rigorous investigation is necessary.
We also found that responders had significantly lower baseline past-year alcohol use scores on the AUDIT-C than non-responders. However, mean scores in these groups were below 3 (the generally accepted threshold for possible abuse or dependence (Bush et al., 1998)), suggesting little evidence of problematic drinking in our sample overall.
While we found no significant association between symptom dimensions and percent change in Y-BOCS or treatment response following IRT, participants who presented with fewer hoarding symptoms were more likely to achieve wellness (Table 5). In agreement with these findings, prior studies of compulsive hoarders have demonstrated poorer treatment outcomes to a variety of treatment approaches including CBT (Abramowitz et al., 2003b; Rufer et al., 2006), behavioral therapy (Mataix-Cols et al., 2002), pharmacologic (Mataix-Cols et al., 1999), intensive multimodal treatment in the context of a partial hospitalization program (Saxena et al., 2002), and limbic surgery (Gentil et al., 2014). Taken together, these findings support the recent view of compulsive hoarding as a distinct disorder separate from OCD that may require different treatment approaches (Pertusa et al., 2010).
In contrast to our prior study, we found no association between sex or level of psychosocial functioning and IRT response. As such, it will be important to expand this research to include IRT populations outside our program in an effort to better understand these contradictory findings.
Characterization of Treatment Course
We found rapid improvement in OCD symptoms over the first 20–30 days of IRT treatment. This finding is consistent with previous studies showing a rapid reduction in OCD symptoms among patients receiving intensive daily outpatient exposure response prevention treatment over a 3–4 week period (Abramowitz et al., 2003a; Foa et al., 2005; Storch et al., 2008) – an approach that closely resembles the behavioral component of IRT. We also found a more gradual decline in OCD symptoms over the subsequent 2 months of IRT, consistent with our initial hypothesis and clinical experience.
Unexpectedly, we found a possible spike in OCD symptoms from days 20–40 and again around day 60 of treatment. Although these spikes may represent statistical artifacts, there is anecdotal clinical experience to support the first spike in symptoms. Several mechanisms could contribute to this so-called “rebound phase”. First, since patients are changing environment to enter IRT, which may mean leaving a home environment that is much more triggering, it is possible that some may experience a “honeymoon period” during the first few weeks of treatment. As new triggers are established in the IRT environment, these patients may experience a worsening of symptoms. Second, due to the significant psychoeducational component of IRT treatment, it is possible that patients uncover previously unrecognized obsessions and/or compulsions over the course of treatment as they become more adept at identifying OCD symptoms. Third, given the step-wise hierarchical nature of ERP treatment which begins with easier exposures and gradually progresses to more challenging ones, it is possible that patients are not habituating as quickly to more difficult exposures as they did earlier in treatment. However, since patients were not receiving a standardized timeline of ERP, which moved patients up their exposure hierarchy only between days 20–40 and after day 60, this explanation is less likely.
Implications for Treatment
Several findings from this study may inform the future delivery of IRT. First, we found that patients with the most severe OCD derived the greatest reduction in symptoms following IRT. This finding contrasts sharply with studies involving outpatient treatment modalities, suggesting that IRT may represent the treatment of choice for severe, treatment-refractory patients. Second, while OCD symptom dimensions do not influence overall symptom reduction or treatment response, patients with fewer hoarding symptoms are more likely to achieve wellness following IRT. Third, greater past-year alcohol use may predict a poorer response to IRT. However, this finding appears unrelated to problematic drinking. Fourth, IRT appears to produce a rapid reduction in OCD symptoms over the first month of treatment, in contrast to outpatient behavioral and pharmacologic treatments for OCD, which typically require 8–12 weeks and often yield modest symptom reduction (Jenike, 2004). As such, IRT may be particularly indicated for patients with severe OCD who require acute intervention to rapidly relieve incapacitating symptoms. Fifth, our data suggest that while patients show rapid improvement over the first month of IRT, this improvement slows in subsequent months and might be disrupted by brief periods of worsening. This finding raises the question of whether the slope of improvement after one month is sufficient to justify the cost of IRT beyond the 30-day mark. Future studies should also assess whether additional interventions, introduced early in treatment, might maintain the steeper trajectory of symptom reduction beyond the first month. One intriguing possibility is the use of d-cycloserine, which has shown preliminary evidence as a pharmacologic enhancer of exposure response prevention therapy for OCD (Kushner et al., 2007; Wilhelm et al., 2008) – primarily through a hastening of the habituation process (Chasson et al., 2010).
Limitations
We acknowledge several limitations to this study. First, we did not include a structured clinical interview on admission, and thus could not include comorbid diagnoses other than depression, post-traumatic stress disorder, and substance use disorders in our analyses of outcome predictors. Given that comorbid mental disorders impact outcome in both cognitive behavior therapy (Keeley et al., 2008) and medication treatment (Baer et al., 1992; Cavedini et al., 1997; Ravizza et al., 1995) in OCD, future studies of IRT treatment predictors should assess for these comorbid conditions. Second, we cannot assess potential “placebo” response (that is, non-specific effects of expectation) in our sample without the inclusion of a control treatment group. A control group would also defend against the “regression to the mean” concern mentioned earlier. Third, while our initial sample was 281 participants, the number of participants providing follow-up data declined steadily over the course of treatment, resulting in a smaller sample with 2 and 3 assessments post-admission. Furthermore, missing data at discharge have the potential to bias the effect of treatment on wellness and response. Thus, future IRT studies examining longitudinal clinical data in larger samples will be necessary. The longitudinal models presented in the present initial study may help to guide such future investigations. Fourth, we did not correct for multiple statistical comparisons so our findings are exploratory and must be interpreted with some caution. Fifth, we did not measure other potentially clinically important variables that have been shown previously to be significant predictors of outcome (such as comorbid tics, level of insight, treatment expectancy, and past number of medication and CBT trials) and therefore could not examine these variables as predictors of outcome. Future research should examine these potential predictors as well as confirm the significant results of this study.
Conclusions
In patients with severe, treatment-refractory OCD, inpatient residential treatment (IRT) was associated with a rapid reduction of OCD symptoms over the first 30 days of treatment and a more gradual decline in symptoms over the remaining 60 days. Individuals with greater baseline OCD severity and less prior alcohol use responded better to IRT while those with fewer hoarding symptoms were more likely to achieve wellness. Future investigations of these issues may help to elucidate the optimal length of stay in the IRT setting, as well as possible interventions to enhance IRT response and achieve overall wellness.
Acknowledgments
We thank Diane Davey, RN, MBA and Evelyn Stewart, MD who played an important role in the conceptualization and initiation of data collection. We also thank Jordan Cattie, Justin Clark, Christina Albano, and Lily Motta who assisted with data collection and management.
ROLE OF THE FUNDING SOURCE
This work was funded in part by Grant 1K23-MH092397 from the National Institute of Mental Health (BPB) and the David Judah Fund at Massachusetts General Hospital (BPB).
Footnotes
CONTRIBUTORS
BPB and JIH designed the study. CL and GMF undertook the statistical analyses. JAE, JMC, BMM, MCA, CMG, and MAJ wrote the protocol for data collection and oversaw all data management. HGP contributed to data analysis and manuscript preparation. BPB wrote the first draft of the manuscript. All authors contributed to and have approved the final manuscript.
CONFLICT OF INTEREST
Dr. Brennan has received research grant support from Eli Lilly and Transcept Pharmaceuticals. Dr. Hudson has received consulting fees from Genentech, HealthCore, Roche, and Shire; and has received research grant support from Genentech, Otsuka, and Shire. None of the other authors report any potential conflicts of interest.
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References
- Abramowitz JS, Foa EB, Franklin ME. Exposure and ritual prevention for obsessive-compulsive disorder: effects of intensive versus twice-weekly sessions. J Consult Clin Psychol. 2003a;71:394–8. doi: 10.1037/0022-006x.71.2.394. [DOI] [PubMed] [Google Scholar]
- Abramowitz JS, Franklin ME, Schwartz SA, Furr JM. Symptom presentation and outcome of cognitive-behavioral therapy for obsessive-compulsive disorder. J Consult Clin Psychol. 2003b;71:1049–57. doi: 10.1037/0022-006X.71.6.1049. [DOI] [PubMed] [Google Scholar]
- Baer L, Jenike MA, Black DW, Treece C, Rosenfeld R, Greist J. Effect of axis II diagnoses on treatment outcome with clomipramine in 55 patients with obsessive-compulsive disorder. Arch Gen Psychiatry. 1992;49:862–6. doi: 10.1001/archpsyc.1992.01820110026003. [DOI] [PubMed] [Google Scholar]
- Bjorgvinsson T, Hart AJ, Wetterneck C, Barrera TL, Chasson GS, Powell DM, Heffelfinger S, Stanley MA. Outcomes of Specialized Residential Treatment for Adults with Obsessive-Compulsive Disorder. J Psychiatr Pract. 2013;19:429–437. doi: 10.1097/01.pra.0000435043.21545.60. [DOI] [PubMed] [Google Scholar]
- Bjorgvinsson T, Wetterneck CT, Powell DM, Chasson GS, Webb SA, Hart J, Heffelfinger S, Azzouz R, Entricht TL, Davidson JE, Stanley MA. Treatment outcome for adolescent obsessive-compulsive disorder in a specialized hospital setting. J Psychiatr Pract. 2008;14:137–45. doi: 10.1097/01.pra.0000320112.36648.3e. [DOI] [PubMed] [Google Scholar]
- Blais MA, Lenderking WR, Baer L, deLorell A, Peets K, Leahy L, Burns C. Development and initial validation of a brief mental health outcome measure. J Pers Assess. 1999;73:359–73. doi: 10.1207/S15327752JPA7303_5. [DOI] [PubMed] [Google Scholar]
- Bloch MH, Landeros-Weisenberger A, Rosario MC, Pittenger C, Leckman JF. Meta-analysis of the symptom structure of obsessive-compulsive disorder. Am J Psychiatry. 2008;165:1532–42. doi: 10.1176/appi.ajp.2008.08020320. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Boschen MJ, Drummond LM, Pillay A. Treatment of severe, treatment-refractory obsessive-compulsive disorder: a study of inpatient and community treatment. CNS Spectr. 2008;13:1056–65. doi: 10.1017/s1092852900017119. [DOI] [PubMed] [Google Scholar]
- Bush K, Kivlahan DR, McDonell MB, Fihn SD, Bradley KA. The AUDIT alcohol consumption questions (AUDIT-C): an effective brief screening test for problem drinking. Ambulatory Care Quality Improvement Project (ACQUIP). Alcohol Use Disorders Identification Test. Arch Intern Med. 1998;158:1789–95. doi: 10.1001/archinte.158.16.1789. [DOI] [PubMed] [Google Scholar]
- Cavedini P, Erzegovesi S, Ronchi P, Bellodi L. Predictive value of obsessive-compulsive personality disorder in antiobsessional pharmacological treatment. Eur Neuropsychopharmacol. 1997;7:45–9. doi: 10.1016/s0924-977x(96)00382-3. [DOI] [PubMed] [Google Scholar]
- Chasson GS, Buhlmann U, Tolin DF, Rao SR, Reese HE, Rowley T, Welsh KS, Wilhelm S. Need for speed: evaluating slopes of OCD recovery in behavior therapy enhanced with d-cycloserine. Behav Res Ther. 2010;48:675–9. doi: 10.1016/j.brat.2010.03.007. [DOI] [PubMed] [Google Scholar]
- Denys D, Burger H, van Megen H, de Geus F, Westenberg H. A score for predicting response to pharmacotherapy in obsessive-compulsive disorder. Int Clin Psychopharmacol. 2003;18:315–22. doi: 10.1097/00004850-200311000-00002. [DOI] [PubMed] [Google Scholar]
- Drummond LM. The treatment of severe, chronic, resistant obsessive-compulsive disorder. An evaluation of an in-patient programme using behavioural psychotherapy in combination with other treatments. Br J Psychiatry. 1993;163:223–9. doi: 10.1192/bjp.163.2.223. [DOI] [PubMed] [Google Scholar]
- Farris SG, McLean CP, Van Meter PE, Simpson HB, Foa EB. Treatment response, symptom remission, and wellness in obsessive-compulsive disorder. J Clin Psychiatry. 2013;74:685–90. doi: 10.4088/JCP.12m07789. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Federici A, Summerfeldt LJ, Harrington JL, McCabe RE, Purdon CL, Rowa K, Antony MM. Consistency between self-report and clinician-administered versions of the Yale-Brown Obsessive-Compulsive Scale. J Anxiety Disord. 2010;24:729–33. doi: 10.1016/j.janxdis.2010.05.005. [DOI] [PubMed] [Google Scholar]
- Foa EB, Liebowitz MR, Kozak MJ, Davies S, Campeas R, Franklin ME, Huppert JD, Kjernisted K, Rowan V, Schmidt AB, Simpson HB, Tu X. Randomized, placebo-controlled trial of exposure and ritual prevention, clomipramine, and their combination in the treatment of obsessive-compulsive disorder. Am J Psychiatry. 2005;162:151–61. doi: 10.1176/appi.ajp.162.1.151. [DOI] [PubMed] [Google Scholar]
- Gentil AF, Lopes AC, Dougherty DD, Ruck C, Mataix-Cols D, Lukacs TL, Canteras MM, Eskandar EN, Larsson KJ, Hoexter MQ, Batistuzzo MC, Greenberg BD, Miguel EC. Hoarding symptoms and prediction of poor response to limbic system surgery for treatment-refractory obsessive-compulsive disorder. J Neurosurg. 2014 doi: 10.3171/2014.2.JNS131423. [DOI] [PubMed] [Google Scholar]
- Goodman WK, Price LH, Rasmussen SA, Mazure C, Fleischmann RL, Hill CL, Heninger GR, Charney DS. The Yale-Brown Obsessive Compulsive Scale. I. Development, use, and reliability. Arch Gen Psychiatry. 1989;46:1006–11. doi: 10.1001/archpsyc.1989.01810110048007. [DOI] [PubMed] [Google Scholar]
- Jenike MA. Clinical practice. Obsessive-compulsive disorder. N Engl J Med. 2004;350:259–65. doi: 10.1056/NEJMcp031002. [DOI] [PubMed] [Google Scholar]
- Karno M, Golding JM, Sorenson SB, Burnam MA. The epidemiology of obsessive-compulsive disorder in five US communities. Arch Gen Psychiatry. 1988;45:1094–9. doi: 10.1001/archpsyc.1988.01800360042006. [DOI] [PubMed] [Google Scholar]
- Keeley ML, Storch EA, Merlo LJ, Geffken GR. Clinical predictors of response to cognitive-behavioral therapy for obsessive-compulsive disorder. Clin Psychol Rev. 2008;28:118–30. doi: 10.1016/j.cpr.2007.04.003. [DOI] [PubMed] [Google Scholar]
- Knopp J, Knowles S, Bee P, Lovell K, Bower P. A systematic review of predictors and moderators of response to psychological therapies in OCD: Do we have enough empirical evidence to target treatment? Clin Psychol Rev. 2013;33:1067–1081. doi: 10.1016/j.cpr.2013.08.008. [DOI] [PubMed] [Google Scholar]
- Kushner MG, Kim SW, Donahue C, Thuras P, Adson D, Kotlyar M, McCabe J, Peterson J, Foa EB. D-cycloserine augmented exposure therapy for obsessive-compulsive disorder. Biol Psychiatry. 2007;62:835–8. doi: 10.1016/j.biopsych.2006.12.020. [DOI] [PubMed] [Google Scholar]
- Mataix-Cols D, Marks IM, Greist JH, Kobak KA, Baer L. Obsessive-compulsive symptom dimensions as predictors of compliance with and response to behaviour therapy: results from a controlled trial. Psychother Psychosom. 2002;71:255–62. doi: 10.1159/000064812. [DOI] [PubMed] [Google Scholar]
- Mataix-Cols D, Rauch SL, Manzo PA, Jenike MA, Baer L. Use of factor-analyzed symptom dimensions to predict outcome with serotonin reuptake inhibitors and placebo in the treatment of obsessive-compulsive disorder. Am J Psychiatry. 1999;156:1409–16. doi: 10.1176/ajp.156.9.1409. [DOI] [PubMed] [Google Scholar]
- Mundt JC, Marks IM, Shear MK, Greist JH. The Work and Social Adjustment Scale: a simple measure of impairment in functioning. Br J Psychiatry. 2002;180:461–4. doi: 10.1192/bjp.180.5.461. [DOI] [PubMed] [Google Scholar]
- Pertusa A, Frost RO, Fullana MA, Samuels J, Steketee G, Tolin D, Saxena S, Leckman JF, Mataix-Cols D. Refining the diagnostic boundaries of compulsive hoarding: a critical review. Clin Psychol Rev. 2010;30:371–86. doi: 10.1016/j.cpr.2010.01.007. [DOI] [PubMed] [Google Scholar]
- Ravizza L, Barzega G, Bellino S, Bogetto F, Maina G. Predictors of drug treatment response in obsessive-compulsive disorder. J Clin Psychiatry. 1995;56:368–73. [PubMed] [Google Scholar]
- Rufer M, Fricke S, Moritz S, Kloss M, Hand I. Symptom dimensions in obsessive-compulsive disorder: prediction of cognitive-behavior therapy outcome. Acta Psychiatr Scand. 2006;113:440–6. doi: 10.1111/j.1600-0447.2005.00682.x. [DOI] [PubMed] [Google Scholar]
- Ruscio AM, Stein DJ, Chiu WT, Kessler RC. The epidemiology of obsessive-compulsive disorder in the National Comorbidity Survey Replication. Mol Psychiatry. 2010;15:53–63. doi: 10.1038/mp.2008.94. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rush AJ, Trivedi MH, Ibrahim HM, Carmody TJ, Arnow B, Klein DN, Markowitz JC, Ninan PT, Kornstein S, Manber R, Thase ME, Kocsis JH, Keller MB. The 16-Item Quick Inventory of Depressive Symptomatology (QIDS), clinician rating (QIDS-C), and self-report (QIDS-SR): a psychometric evaluation in patients with chronic major depression. Biol Psychiatry. 2003;54:573–83. doi: 10.1016/s0006-3223(02)01866-8. [DOI] [PubMed] [Google Scholar]
- Saxena S, Maidment KM, Vapnik T, Golden G, Rishwain T, Rosen RM, Tarlow G, Bystritsky A. Obsessive-compulsive hoarding: symptom severity and response to multimodal treatment. J Clin Psychiatry. 2002;63:21–7. [PubMed] [Google Scholar]
- Shetti CN, Reddy YC, Kandavel T, Kashyap K, Singisetti S, Hiremath AS, Siddequehusen MU, Raghunandanan S. Clinical predictors of drug nonresponse in obsessive-compulsive disorder. J Clin Psychiatry. 2005;66:1517–23. doi: 10.4088/jcp.v66n1204. [DOI] [PubMed] [Google Scholar]
- Skinner HA. The drug abuse screening test. Addict Behav. 1982;7:363–71. doi: 10.1016/0306-4603(82)90005-3. [DOI] [PubMed] [Google Scholar]
- Stein DJ, Montgomery SA, Kasper S, Tanghoj P. Predictors of response to pharmacotherapy with citalopram in obsessive-compulsive disorder. Int Clin Psychopharmacol. 2001;16:357–61. doi: 10.1097/00004850-200111000-00007. [DOI] [PubMed] [Google Scholar]
- Stewart SE, Stack DE, Farrell C, Pauls DL, Jenike MA. Effectiveness of intensive residential treatment (IRT) for severe, refractory obsessive-compulsive disorder. J Psychiatr Res. 2005;39:603–9. doi: 10.1016/j.jpsychires.2005.01.004. [DOI] [PubMed] [Google Scholar]
- Stewart SE, Stack DE, Tsilker S, Alosso J, Stephansky M, Hezel DM, Jenike EA, Haddad SA, Kant J, Jenike MA. Long-term outcome following Intensive Residential Treatment of Obsessive-Compulsive Disorder. J Psychiatr Res. 2009;43:1118–23. doi: 10.1016/j.jpsychires.2009.03.012. [DOI] [PubMed] [Google Scholar]
- Stewart SE, Yen CH, Stack DE, Jenike MA. Outcome predictors for severe obsessive-compulsive patients in intensive residential treatment. J Psychiatr Res. 2006;40:511–9. doi: 10.1016/j.jpsychires.2005.08.007. [DOI] [PubMed] [Google Scholar]
- Storch EA, Larson MJ, Shapira NA, Ward HE, Murphy TK, Geffken GR, Valerio H, Goodman WK. Clinical predictors of early fluoxetine treatment response in obsessive-compulsive disorder. Depress Anxiety. 2006;23:429–33. doi: 10.1002/da.20197. [DOI] [PubMed] [Google Scholar]
- Storch EA, Merlo LJ, Lehmkuhl H, Geffken GR, Jacob M, Ricketts E, Murphy TK, Goodman WK. Cognitive-behavioral therapy for obsessive-compulsive disorder: a non-randomized comparison of intensive and weekly approaches. J Anxiety Disord. 2008;22:1146–58. doi: 10.1016/j.janxdis.2007.12.001. [DOI] [PubMed] [Google Scholar]
- Tukel R, Bozkurt O, Polat A, Genc A, Atli H. Clinical predictors of response to pharmacotherapy with selective serotonin reuptake inhibitors in obsessive-compulsive disorder. Psychiatry Clin Neurosci. 2006;60:404–9. doi: 10.1111/j.1440-1819.2006.01523.x. [DOI] [PubMed] [Google Scholar]
- Wilhelm S, Buhlmann U, Tolin DF, Meunier SA, Pearlson GD, Reese HE, Cannistraro P, Jenike MA, Rauch SL. Augmentation of behavior therapy with D-cycloserine for obsessive-compulsive disorder. Am J Psychiatry. 2008;165:335–41. doi: 10.1176/appi.ajp.2007.07050776. quiz 409. [DOI] [PubMed] [Google Scholar]
- Wilhelm S, Steketee G. Cognitive therapy for obsessive-compulsive disorder: A guide for professionals. Oakland, CA: New Harbinger Publications; 2006. [Google Scholar]
- Yovel I, Gershuny BS, Steketee G, Buhlmann U, Fama JM, Mitchell J, Wilhelm S. Idiosyncratic Severity Profiles of Obsessive Compulsive Dysfunction: A Detailed Self Report Assessment of a Multifaceted Syndrome. Cogn Ther Res. 2012;36:694–713. [Google Scholar]